Tracheobronchial anomalies in chromosome 22q11.2 microdeletion

Am J Med Genet A. 2006 Apr 1;140(7):790-3. doi: 10.1002/ajmg.a.31155.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Bronchi / abnormalities*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • Face / abnormalities
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant, Newborn
  • Karyotyping
  • Syndrome
  • Trachea / abnormalities*